S13N (p.Ser13Asn) variant of CD28 (P10747)
S13N (p.Ser13Asn) in CD28 (P10747) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.34 / 1. The record also includes population frequency data, published literature, and structural context.
S13N (p.Ser13Asn) variant details
- p.Ser13Asn
- rs769258035
- gnomAD 2-203706540-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.341
- CADD 11.50
- SIFT 0.28
- Population evidence available
- Structural context available
- Literature evidence available